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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2093003Generated: November 4, 2026

(3-Chloro-5-methoxyphenyl)methanol → 3-Chloro-5-methoxybenzaldehyde

https://huagongshe.com/reaction/2093003

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(3-Chloro-5-methoxyphenyl)methanolHCID 12909342—
ReactantHCID 178418287HCID 178418287—
SolventDiethyl EtherHCID 3283—
Product3-Chloro-5-methoxybenzaldehydeHCID 2190463378%

Reaction Steps

A mixture of 3-chloro-5-methoxybenzyl alcohol (5.0 g, 28.9 mmol) and pyridinium chlorochromate (20% on alumina, 40 g, 37.8 mmol) was allowed to stir for 1.25 hr. Diethyl ether (200 ml) was then added followed by filtration of precipitate. The filtrate was concentrated under reduced pressure and the resulting residue was purified via silica gel chromatography using 40% dichloromethane, 60% petroleum ether as eluant, to give 3.8 g of 3-chloro-5-methoxybenzaldehyde (78%). 1H-NMR (CDCl3): 3.84 (s, 3H) 7.13 (s, 1H), 7.28 (s, 1H), 7.41 (s, 1H), 9.89 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08440706B2
Source datasetuspto-grants-2013_05
ORD IDord-0f951a0640a14e9994e37310716f99ea
Source noteuspto-grants-2013_05